NM_004713.6(NEMF):c.578A>G (p.Tyr193Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002717552.2
Allele description [Variation Report for NM_004713.6(NEMF):c.578A>G (p.Tyr193Cys)]
NM_004713.6(NEMF):c.578A>G (p.Tyr193Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Polymorphobacter fuscus strain D40P Scaffold6, whole genome shotgun sequence
Polymorphobacter fuscus strain D40P Scaffold6, whole genome shotgun sequencegi|1774037440|ref|NZ_WIOL01000006.1 |WGS:NZ_WIOL01|Scaffold6Nucleotide
-
HG03190 AND estd219 (4079)
dbVar
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Last Updated: May 1, 2024